U.S. patent application number 10/146420 was filed with the patent office on 2004-05-27 for synthesis of stable colloidal nanocrystals using organic dendrons.
Invention is credited to Chen, Haiyan, Peng, Xiaogang.
Application Number | 20040101976 10/146420 |
Document ID | / |
Family ID | 28044309 |
Filed Date | 2004-05-27 |
United States Patent
Application |
20040101976 |
Kind Code |
A1 |
Peng, Xiaogang ; et
al. |
May 27, 2004 |
Synthesis of stable colloidal nanocrystals using organic
dendrons
Abstract
A method for stabilizing colloidal suspensions of nanocrystals
or nanoparticles in a solvent or solid matrix is provided by
coating the nanocrystals with bulky organic molecules, specifically
dendrons. By coating nanocrystals with a dense organic dendron coat
and further cross-linking the dendron ligands, oxidation of the
nanocrystals and dissociation of the ligands are avoided. This
invention allows nanocrystals to undergo rigorous purification and
processing. It may regularly be applied to a variety of
nanocrystals.
Inventors: |
Peng, Xiaogang;
(Fayetteville, AR) ; Chen, Haiyan; (Fayetteville,
AR) |
Correspondence
Address: |
JOHN S. PRATT, ESQ
KILPATRICK STOCKTON, LLP
1100 PEACHTREE STREET
SUITE 2800
ATLANTA
GA
30309
US
|
Family ID: |
28044309 |
Appl. No.: |
10/146420 |
Filed: |
May 13, 2002 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
60290541 |
May 14, 2001 |
|
|
|
Current U.S.
Class: |
436/525 ;
525/54.1 |
Current CPC
Class: |
C01B 19/007 20130101;
C30B 5/00 20130101; C30B 29/605 20130101; C30B 33/00 20130101 |
Class at
Publication: |
436/525 ;
525/054.1 |
International
Class: |
C08H 001/00; G01N
033/553 |
Claims
What is claimed is:
1. A method for stabilizing a nanoparticle in a solution or solid
matrix comprising: covalently binding a plurality of ligands to a
nanoparticle; wherein each of said ligands has a nanoparticle
binding site and at least one active site.
2. The method of claim 1 wherein said nanoparticle is a
nanocrystal.
3. The method of claim 1 wherein said ligand is a dendron having a
plurality of active sites.
4. The method of claim 1 further comprising the cross linking of
said active sites of said ligands.
5. The method of claim 4 wherein said crosslinking of said active
sites includes the addition of a crosslinking agent.
6. The method of claim 1 wherein said at least one active site of
said ligands are hydrophobic.
7. The method of claim 1 wherein said at least one active site of
said ligands are hydrophilic.
8. The method of claim 1 wherein said nanoparticle is comprised of
a material selected from the group consisting of inorganic elements
and inorganic-compounds.
9. The method of claim 8 wherein said nanoparticle is comprised of
a material selected from the group consisting of gold, silver
platinum, copper, iridium, palladium, silicon, germanium, iron,
cobalt, nickel, iron oxide, cobalt oxide, nickel oxide, titanium
oxide, zinc oxide, cadmium selenide, cadmium sulfide, cadmium
telluride, zinc sulfide, zinc selenide, zinc telluride, mercury
sulfide, mercury selenide, mercury telluride, indium phosphorus,
indium arsenide, indium nitride, gallium arsenide, gallium
phosphide, gallium nitride, gallium selenide, gallium sulfide,
indium selenide, indium sulfide and indium telluride.
10. The method of claim 1 wherein said nanoparticle is comprised of
a combination of elements from group IV, groups II and VI or groups
III and V of the periodic table.
11. The method of claim 1 wherein said at least one active site is
selected from the group consisting of hydroxyl groups, amine
groups, ethylene groups, dipyridine groups, carboxylic acid groups,
carbonyl groups, halide groups and ester groups.
12. The method of claim 1 wherein said nanocrystal binding site is
selected from the group consisting of thiol, carboxylic acid,
amine, hydroxylamide, phosphine, phosphine oxide, and phosphonic
acid.
13. A stable nanoparticle in a solution or solid matrix comprising:
a plurality of ligands covalently bound to a nanoparticle; wherein
each of said ligands has a nanoparticle binding site and at least
one active site.
14. The stable nanoparticle of claim 13 wherein said nanoparticle
is a nanocrystal.
15. The stable nanoparticle of claim 13 wherein said ligand is a
dendron having a plurality of active sites.
16. The stable nanoparticle of claim 13 wherein said active sites
of said ligands are chemically cross linked.
17. The stable nanoparticle of claim 16 further comprising a
crosslinking agent.
18. The stable nanoparticle of claim 13 wherein said at least one
active site of said ligands are hydrophobic.
19. The stable nanoparticle of claim 13 wherein said at least one
active site of said ligands are hydrophilic.
20. The stable nanoparticle of claim 13 wherein said nanoparticle
is comprised of a material selected from the group consisting of
gold, silver platinum, copper, iridium, palladium, silicon,
germanium, iron, cobalt, nickel, iron oxide, cobalt oxide, nickel
oxide, titanium oxide, zinc oxide, cadmium selenide, cadmium
sulfide, cadmium telluride, zinc sulfide, zinc selenide, zinc
telluride, mercury sulfide, mercury selenide, mercury telluride,
indium phosphorus, indium arsenide, indium nitride, gallium
arsenide, gallium phosphide, gallium nitride, gallium selenide,
gallium sulfide, indium selenide, indium sulfide and indium
telluride.
21. The stable nanoparticle of claim 13 wherein said nanoparticle
is comprised of a combination of elements from the noble metals,
transition metals, metal oxides, metal halides, group IV, groups II
and VI or groups III and V.
22. The stable nanoparticle of claim 13 wherein said at least one
active site is selected from the group consisting of hydroxyl
groups, amine groups, ethylene groups, dipyridine groups,
carboxylic acid groups, carbonyl groups, halide groups and ester
groups.
23. The stable nanocrystal of claim 13 wherein said nanocrystal
binding site is selected from the group consisting of thiol,
carboxylic acid, hydroxylamide, phosphine, amine, phosphine oxide,
and phosphonic acid.
24. A biomedical detection reagent comprising: a stable nanocrystal
produced by the method of claim 1, a compound designed to detect a
biological analyte, wherein said nanocrystal and said compound are
covalently coupled to each other.
25. The reagent of claim 24 wherein said compound is a antibody for
use in an immunoassay.
26. The reagent of claim 24 wherein said compound is a
polynucleotide probe for use in a polynucleotide hyrbridization
reaction.
27. A laser or LED comprising a stable nanoparticle produced by the
method of claim 1 wherein said nanoparticle emits photo-radiation
upon photo or electronic excitation.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This U.S. utility Patent Application claims priority to U.S.
Provisional patent application No. 60/290,541, filed on May 14,
2001.
STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT
[0002] Not applicable.
REFERENCE TO A SEQUENCE LISTING A TABLE, OR A COMPUTER PROGRAM
LISTING COMPACT DISC APPENDIX
[0003] Not applicable.
BACKGROUND OF THE INVENTION
[0004] 1. Field of the Invention.
[0005] The present invention relates to the use of organic ligands
to stabilize nanocrystal colloids in solution. More specifically,
the present invention relates to the use of ligands, especially
cross linked ligands, to prevent oxidation, deterioration,
precipitation and segregation of nanocrystals in a colloidal
suspension or solid matrix.
[0006] 2. Prior Art.
[0007] Nanotechnology is one of the fastest growing fields in the
industry. Microscopic devices have countless applications.
Currently, the chemistry behind synthesis and processing of
nanomaterials are the two key areas of research scientists are
focusing on. Once nanomaterials can be readily synthesized and
processed, almost any device could be formed on a nanoscopic
scale.
[0008] Colloidal nanocrystals are nanometer sized fragments of
corresponding bulk crystals dispersed in solvents or other types of
matrices. They are one of the many materials being explored for a
variety of applications because of their novel, size dependent
properties and potentially flexible processing chemistry. In some
cases, the nanometer sized particles may not be crystalline
materials. Nanocrystals and nanoparticles show promise for use as
light emitting diodes (LEDs), labels for bioassays and a host of
other applications. Recent progress in the synthesis of high
quality of nanocrystals, especially chalcogenides nanocrystals for
use as semiconductors, as highlighted the need for methods for
maintaining and handling these nanocrystals. Adequate methods of
processing nanocrystals are essential for utilizing them in
nanodevices and other nanostructures. For example, the size
dependent emission properties of semiconductor nanocrystals make
them highly desirable as labeling reagents for biomedical
applications and as color tunable emitting materials in LEDs and
lasers.
[0009] Compared to conventional photoluminescence-based labeling
reagents, semiconductor nanocrystals possess many invaluable
advantages. With their very narrow but size-dependent band-edge
emission spectrum and their extremely broad absorption spectrum,
semiconductor nanocrystals simplify the current detection scheme
significantly. The emission of semiconductor nanocrystals can last
magnitudes longer than that of conventional organic dyes under
optical radiation. By simply tuning the size of very few kinds of
semiconductor nanocrystals, the detection window can cover the same
wavelength range of tens of different organic dyes.
[0010] In addition, conjugation chemistry for coupling different
sizes/types of semiconductor nanocrystals with bio-functional
species can potentially be the same because the coupling reactions
always occur on the outer surface of the ligand layer. This has
already been shows with cadmium selenide nanocrystals having a zinc
sulfite shell and a thiol-silica ligand layer. Unfortunately, this
process is very difficult to reproduce and the resulting
nanocrystals deteriorate rapidly and are not well suited for
subsequent purification procedures.
[0011] Ligands on the surface of colloidal nanocrystals, sometimes
also called capping groups or surfactants, etc., are certain types
of organic molecules with two distinguishable parts. One part of
the molecule can chemically bind to the surface of the inorganic
nanocrystals (or nanoparticles), and the other part helps the
nanocrystals (or nanoparticles) to be dispersible in solvents or
matrices.
[0012] Nanocrystals often precipitate out of solution because of
the loss of their thiol ligands. One method of alleviating this
problem is to use di-thiol ligands to increase stability.
Unfortunately, the process is still difficult and the nanocrystals
still deteriorate relatively rapidly.
[0013] One of the significant problems with nanocrystals is their
tendency to rapidly oxidize and loose their unique properties.
Another difficulty with nanocrystals is their low solubility. Die
to their size, they must be held in a colloidal suspension, and are
by their very nature insoluble. The use of thiol ligands has been
an attempt to solve both of these problems.
[0014] By attaching ligands to the surface of the nanocrystals, it
has been hoped that this would sterically hinder oxidation. While
ligands do have a slight impact on oxidation, they have to date
been unable to give nanocrystals the stability necessary for
desired applications.
[0015] Similarly, ligands have so far proved disappointing in being
able to maintain a colloidal suspension of nanocrystals. Functional
groups having desired hydrophobic or hydrophilic properties have
been attached to the ends of the ligands and do in fact aid to
maintain a colloidal suspension. However, because the ligands
dissociate, the colloids have a relatively short life time.
[0016] It is therefore desirable to provide a method of maintaining
a colloidal suspension of nanocrystals for a very long time.
[0017] It is also desirable to provide a method for preventing
oxidation of nanocrystals.
SUMMARY OF THE INVENTION
[0018] In the present invention, dendron ligands are attached to a
nanocrystal or nanoparticle and may be subsequently cross linked.
By cross linking the ligands, they are more tightly held about the
nanocrystal and dissociation is prevented. In addition, the cross
linking of the bulky dendron ligands prevents oxygen molecules from
getting close enough to the nanocrystal to facilitate
oxidation.
[0019] Dendrons are hyper-branched organic molecules with a focal
point. In this invention, the focal point is used as the binding
site to the surface of inorganic nanocrystals, or nanoparticles.
Typically, dendrons only refer to molecules having regular branched
structures. However, in this invention, dendrons also include
molecules that are irregularly branched.
[0020] In the present invention it is preferred to use
multi-branched dendrons rather than more common single chair
ligands. A multi branched dendron possesses many advantages over
single chain ligands. The additional mass greatly enhances the
protection against oxidation. It also increases the number of
functional groups that interact with the solution in order to
suspend the nanocrystal. Another advantage is that it provides
additional functional groups for cross linking.
[0021] Because each dendron ligand possesses several functional
groups capable of cross linking, there is no need to the cross
linking reaction to completion. With only one or two functional
groups cross linked with a neighboring dendron ligand, oxidation
rate greatly decreases and dissociation is avoided. Nanocrystals
protected by the present invention will last indefinitely if the
inorganic nanocrystal ores are chemically stable in a given
environment. In addition, they will readily survive the rigorous
processing and purification methods necessary for some applications
such as biomedical labeling.
[0022] It is therefore an object of the present invention to
provide a method of reducing oxidation of a nanocrystal in
solution.
[0023] It is another object of the present invention to provide a
method a method for forming colloidal suspension of nanocrystals
having long term stability.
BRIEF DESCRIPTION OF THE DRAWINGS
[0024] FIG. 1 shows the diagrammatic illustration of a dendron
protected nanocrystal.
[0025] FIG. 2 is a diagrammatic illustration of a ligand protected
nanocrystal and a dendron protected nanocrystal.
[0026] FIG. 3 shows a diagrammatic illustration of a dendron
cross-linking reaction for the present invention.
[0027] FIG. 4 shows a diagrammatic illustration of an alternative
cross linking reaction for the present invention.
[0028] FIG. 5 shows a diagrammatic illustration of an alternative
cross linking method for the present invention.
[0029] FIG. 6 shows a diagrammatic illustration of various ligands
utilized to protect nanocrystals.
[0030] FIG. 7 shows a graph illustrating the effectiveness of
dendrons for protecting nanocrystals.
[0031] FIG. 8 shows IR spectrums illustrating the effectiveness of
an amide coupling reaction.
[0032] FIG. 9 shows the IR spectra of dendron protected
nanocrystals compared to dendrons alone.
[0033] FIG. 10 shows the results of a gel-electrophoresis assay of
dendron protected nanocrystals before and after two different
chemical reactions.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0034] The present invention is directed to the development of
organic dendron ligands and other bulky molecules, which improve
the stability of colloidal suspensions of inorganic nanocrystals.
Because of the steric crowding characteristics and wide variety of
complex secondary/tertiary structures of these molecules, these
ligands may be densely packed and cross linked to form a dense,
compact ligand layer completely coating a nanocrystal. These
dendron protected nanocrystals (DP-nanocrystals) form highly stable
nanocrystal colloidal suspension. Furthermore, these
DP-nanocrystals are stable enough to readily withstand coupling
reactions and purification and separation techniques required for
biomedical and other applications. Those skilled in the art will
appreciate that by changing the functional groups at the
nanoparticle binding sites (NBS's) and active sites, it is possible
to apply these protective ligands to any type of nanocrystal in any
type of solution or solid matrix.
[0035] "Nanocrystal" refers to a nanometer-scale crystalline
particle. While the invention is described in terms of
nanocrystals, the invention may be used for the stabilization of
any nanoparticle, whether it is crystalline or not. Those skilled
in the art will appreciate that so long as there is a suitable
functional group capable of covalently attaching to the
nanoparticle at the focal point of the dendron.
[0036] "Ligand" refers to molecules having one or more chains that
are used to stabilize nanoparticles. Ligands have a focal point on
one end where it binds to the nanoparticle, and at least one active
site that either interacts with the surrounding environment,
cross-links with other active sites, or both.
[0037] "Active site" refers to sites on the ligand designed to
perform one or two functions. They are generally located at the
ends of chains furthest from the nanoparticle or nanocrystal being
stabilized. Active sites are partially determined by the
environment into which the nanocrystal is placed. E.g., polar
active sites are used in polar environments.
[0038] "Nanoparticle binding site," "nanocrystal binding site" and
"NBS" refer to the focal point of a ligand that covalently binds to
a nanoparticle or nanocrystal.
[0039] The present invention results from the discovery that the
packing density of the ligand layer surrounding a nanocrystal plays
a key role in determining the stability of the nanocrystal. CdSe
nanocrystals coated with single chain thiol ligands were studied
first. The results demonstrated that the stability of the thiol
coated CdSe nanocrystals is not associated with the electron
donating ability of the thiol group. Therefore, di-thiol ligands do
not improve the photochemical and chemical stability of
nanocrystals, because they have a greater tendency to form
disulfides through intra-molecular reactions. For single chain
hydrocarbon thiol ligands, the photochemical, chemical and thermal
stabilities of the nanocrystal-ligand complexes is determined
solely by the length of the hydro carbon chain. The results further
show that the thin ligand coat stabilizes the system by slowing
down the diffusion of small molecules such as O.sub.2 into the
inner interface between the nanocrystal and its ligands. The same
results were also observed for thiol coated gold nanocrystals.
[0040] The discovery that additional side chains on ligands or
other bulky molecules that add significant mass to the ligand
protein is the driving force behind stability of colloidal
suspensions of nanocrystals resulted in the present invention.
While adding bulk for mass alone greatly improves the stability of
colloidal suspensions of nanocrystals it has been further
discovered that by cross linking the multi-chained ligands, the
stability of the nanocrystals was further enhanced by at least an
order of magnitude.
[0041] Organic dendron ligands are regularly hyper-branched organic
molecules (examples in FIG. 6) with a central focal point which is
used as the binding site for the anionic/metallic elements on the
surface of nanocrystals. The number of the branching points along
one chain from the focal point to the outer terminal group is the
generation number of the dendrons. There are two reasons to choose
organic dendron ligands. First of all, their steric crowding
characteristics may provide a closely packed but thin ligand shell
which may be as efficient as a shell formed by the ligands with a
long and floppy single chain. Importantly, the steric crowding of a
dendron is very ideal for filling the ligand layer because the
dendron ligands can naturally pack in a cone shape on the surface
of nanocrystals. Secondly, the inter- and intra-molecular chain
tangling of the dendrons with relatively flexible branches may
further slow down the diffusion of small molecules or ions from the
bulk solution into the interface between a nanocrystal and its
ligands. FIG. 2 shows a schematic comparison for the diffusion of
O.sub.2 from the bulk solution into the inner interface between a
nanocrystal and its ligand shell in the cases of simple ligands and
dendron ligands. A similar mechanism was actually proposed to
explain the improved photoluminescence efficiency of organic dyes
encapsulated inside dendrimers.
[0042] FIG. 1 shows a diagrammatic illustration of a
DP-nanocrystal. Nanocrystal 22 may be comprised of any of a number
of inorganic compounds. It may be a combination of elements from
groups II and VI or a combination of elements from groups III and V
of the periodic table, for example, CdSe or InP. It may also be a
noble medal, transition metals, metal oxides, etc. Those skilled in
the art will appreciate that these are some of the more common
nanocrystals. Those skilled in the art will also appreciate that
any nanocrystal that is readily grown in a laboratory may be
suitable for the present invention.
[0043] Dendrons 24 have NBS's 26 which covalently bind to
nanocrystal 22. NBS 26 may be any of a number of functional groups.
Those skilled in the art will appreciate that generally
nucleophyllic functional groups are most suitable to binding to
nanocrystals, i.e. Negatively charged or electron donating
functional groups tend to be the best suited for binding to
crystals. It is known in the art that thiol functioning groups are
very well suited for most compound semiconductor and nobel metals
for this purpose. Those skilled in the art will appreciate that
both thiol and amine functional groups are particularly well suited
for semiconductor nanocrystals especially nanocrystals formed by
combinations of elements from groups II and VI or III and V of the
periodic table. Thiol NBS groups are also well suited for binding
to noble metal nanocrystals. For magnetic nanocrystals, such as
iron oxide, iron, cobalt and nickel, NBS's comprised of a
carboxylic acid, carboxyl or hydroxyamime functional groups are
preferred.
[0044] Dendrons 24 are organic molecules having multiple branching
chains. Dendrons may be formed by any of a variety of organic
compounds known in the art. In this particular embodiment, dendrons
24 have 4 branches. Generally, the more branches of a dendron, the
more effective it is at stabilizing and protecting a nanocrystal.
Those skilled in the art will appreciate that the more branches
dendron 24 has, the more steric hindrance it provides against
smaller molecules. The more bulk there is to the dendron, the more
difficult it is for oxidizing agents to reach the nanocrystal and
oxidize it. This also prevents oxidizing agents from reacting with
NBS 26 and causing dendron 24 to dissociate. Ligands having only a
single chain are known in the art to be generally ineffective. It
was previously believed that the ineffectiveness of single chain
ligands was due primarily to instability of the thiol NBS's. One of
the significant features of the present invention is the discovery
that the ineffectiveness of single chain ligands is largely due to
their inability to effectively coat a nanocrystal. By utilizing
ligands having multiple chains such as dendrons 24, much greater
protection is provided for the nanocrystal. In addition, multi
chain dendrons protect their own NDS alleviating any instability in
their covalent bonds to the nanocrystal by blocking agents that
would dissociate them. This is a vast improvement over the previous
attempts which involved adding thiol groups to the ligand.
[0045] At the ends of dendron's 24 branches, active sites 30 are
located. Active sites 30 preferably perform two functions. First,
they interact with the immediate environment, that is, the solution
in which the nanocrystals are suspended. If the nanocrystals are
placed in an aqueous solution or solid matrix, active sites 30 are
preferably hydrophilic. Alternatively, if the nanocrystals are
placed in an oily solvent, active sites 30 would be preferably
hydrophobic. Those skilled in the art will appreciate that the
nature of the solution will determine what active site is
desired.
[0046] Second, active sites 30 preferably interact with each other
in order to cross link dendrons 24. Those skilled in the art will
appreciate that there are a large variety of cross linking
functional groups, only a few of which will be described herein.
Another important aspect of the present invention is the use of
active sites 30 to cross link dendrons 24. This causes dendrons 24
to form a densely packed coating about nanocrystal core 22. The
cross linking acts synergistically along with multi chain dendrons
to further stabilize nanocrystal 22. The tight packing of the
dendron coating significantly enhances the resistance of the
nanocrystal-ligand complexes to oxidizing agents and other
deleterious molecules that cause either deterioration or
dissociation. Furthermore, even if a dendron's NBS looses its
covalent bond to nanocrystal 22, it will not fall into solution,
but will rather remain part of the dendron coating. This is because
the dendron is also covalently bound to neighboring dendrons my
means of cross linked active sites. By using cross linked, multi
chained dendrons to coat a nanocrystal, the problems found in the
prior art are essentially eliminated.
[0047] FIG. 2 illustrates the advantages of using multi chain
dendrons. Nanocrystal 36 is protected by single chain ligands 40.
Alternatively, dendron protected nanocrystal 38 is protected by
multi chain dendrons 42. Ligands 40 are insufficient to sterically
hinder oxidizing agent 44. Even though dendrons 42 are not cross
linked, their bulk blocks agents 44 from reaching the surface of
nanocrystal 46. Single chain ligands 40 lack the bulk to sterically
hinder agents 44 which readily reach the surface of nanocrystal 48.
Although not shown in this illustration, it is generally preferred
to cross link dendrons 42.
[0048] Cross-linking of dendron ligands is generally accomplished
by the formation of relatively strong molecular interactions.
Cross-linking methods other than hydrogen bonding and electrostatic
interactions require cross-linking reagents. For the formation of
inorganic complexes, inorganic ions are used as the cross-linking
reagents. Cross-linking can also be performed by using those
cross-linking reagents which can form multiple covalent bonds with
the active sites of different ligands. FIG. 3 shows one simple
example of such multi-functional cross-linking reagents. If it is
necessary, multiple cross-linking strategies may be applied.
[0049] FIG. 3 illustrates one such cross linking reaction. DP
nanocrystal 50 is protected by dendrons 52. Dendrons 52 have active
sites 54 comprised of hydroxyl groups. Cross linker 56 is added to
the solution in which nanocrystal 50 is suspended. Cross linker 56
interacts with the hydroxyl groups of active sites 54 to result in
cross links 58. For simplicity, FIG. 3 shows only a partial ligand
coating on nanocrystal 50. Another advantage of using a multi
chained dendron is that it is unnecessary to carry the cross
linking reaction to 100% completion. Because each dendron has
multiple active sites, the cross linking reaction that only reaches
partial completion will sufficiently cross link the dendron ligands
on the surface of a nanocrystal. The cross linking reaction
illustrated in FIG. 3 is well suited for nanocrystals in a
hydrophilic environment. If single chain, ligands are used, unless
100% completion of the cross linking reaction is achieved, it
results in a ligand coat that may still partially dissociate and
cause the nanocrystal to deteriorate. Single chain ligands can be
sufficiently cross-linked by applying multi-step cross-linking, or
using ligands capable of multi-cross-linking reactions, such as
covalent bonding as shown in FIG. 3 and complex formation as shown
in FIG. 5. Therefore, the present invention may be applied to
stabilization via single chain ligands.
[0050] FIG. 4 is a partial illustration of a DP nanocrystal
suitable for suspension in hydrophobic solutions. DP nanocrystals
60 is comprised of a nanocrystal 62 having dendrons 64 bound to it.
Active sites 66 of dendrons 64 are comprised of ethylene groups.
Those skilled in the art will appreciate that if a Grubbs catalyst
is combined DP nanocrystals 60 it will catalyze a reaction causing
active sites 66 to cross link, thus forming cross links 68. This
results in the formation of a hydrophobic dendron coat about
crystal 62.
[0051] FIG. 5 is a partial illustration of another method of
protecting nanocrystals with cross linked dendrons. DP nanocrystal
70 is comprised of nanocrystal 72 having covalently bound dendrons
74. Dendrons 74 have active sites 76 comprised of bipyridine. When
these DP nanocrystals are combined with ruthenium or other
transition metal ions, neighboring bipyridine active sites form a
cross linking complex 80 with the ruthenium. Cross linking
complexes 80 are highly stable. Those skilled in the art will be
familiar with the bipyridine/Ru.sup.3+ complex and other types of
complexes suitable for this purpose. However, this is the first
instance in which this complex has been designed to cross link
dendron ligands on the surface of colloidal nanocrystals.
[0052] The thiol group is a preferred NBS because of its versatile
coordination chemistry to semiconductor and noble metal
nanocrystals. For the biomedical applications of colloidal
semiconductor and nobel metal nanocrystals, the outer terminal
groups of the dendron ligands may be amides, carboxylic acids,
alcohols or esters, which resemble that of a hydrophilic protein or
a sugar. The branches of a dendron ligand may not be completely
symmetric, because it may potentially provide better steric
crowding efficiency over the entire ligand shell and a more
efficient coupling reaction. Experimental results indicate that the
dendron ligands described in this paragraph work well for
differently sized CdSe nanocrystals and gold nanocrystals dispersed
in water and polar solvents.
[0053] Photochemical, thermal and chemical stability of the
DP-nanocrystals is exceptionally good in comparison to the
nanocrystals coated by single-chain thiol ligands. For
semiconductor nanocrystals, such as CdSe nanocrystals, the
normalized OD at the original excitation absorption peak of the
nanocrystals was used as the indicator of the photo-oxidation of
the nanocrystals. FIG. 7 illustrates that the photochemical
stability of the CdSe nanocrystals increases with the increase of
the number of the generation of the dendron ligands with a similar
structure. The molecular structure of the thiol dendrons are
illustrated in FIG. 6. Without additional UV radiation, the aqueous
solution of G2 and G3 dendron-nanocrystals after removing excess
ligands can be stored under ambient conditions for at least several
months without any precipitation. As described below, this
exceptional stability of the CdSe nanocrystals coated by the G2 or
G3 dendrons is sufficient for necessary coupling and purification
procedures.
[0054] Previously reported results reveal that the photochemical
stability of nanocrystal/ligand complexes can be improved
significantly by simply increasing the molecular weight of the
single chain ligands. That is so because the longer the chain is,
the thicker the ligand layer will be. For this reason, it was
important to verify that the improved stability of
dendron-nanocrystals is not simply caused by the increase of the
molecular weight of the dendrons. Three ligands with different
degrees of branches but with a similar molecular weight shown in
FIG. 6 were studied to clarify this issue. The experimental results
indicated that the stability of the CdSe nanocrystal/ligand
complexes is strongly associated with the degree of the branching
of the ligands.
[0055] Gold nanocrystals coated by single-chain thiols, such as
MUA, are generally very fragile. They can not withstand
precipitation by sodium chloride solution and the resulting
precipitate is insoluble in pure water. They have to be purified by
ultracentrifuge that does not convert the nanocrystal/ligand
complex into solid/powder form. In contrast, the gold
dendron-nanocrystals can be precipitated by sodium chloride
solution and be re-dispersed in water repeatedly. In general, the
gold DP-nanocrystals are more stable against photo-oxidation than
the corresponding CdSe dendron-nanocrystals.
[0056] For biological applications, it is essential that
nanocrystal/ligand complexes should be stable enough for certain
types of coupling reactions which conjugate biologically active
species to the nanocrystal/ligand complex. Amide coupling of the
dendron-nanocrystals through either the ester-amine coupling or the
traditional EDC coupling works well. Several types of primary
amines, such as glycineamide, 2-aminoacetonitrile, benzylamine,
2-aminoethanol and ammonia were successfully coupled to the outer
surface of the DP-nanocrystals. The solubility of the
DP-nanocrystals is largely dependent on the resulting amide. For
example, the ester terminated CdSe dendron-nanocrystals were only
soluble in organic solvents. After reacting with ammonia or
2-aminoethanol, the dendron-nanocrystals became only soluble in
water. Infrared (IR) and H.sup.1 NMR studies revealed that the
ester-amine coupling reaction could be close to 100% completion.
The ester stretching vibration band at around 1740 cm.sup.-1 and
the methyl deformation mode at 1370 cm.sup.-1 disappeared
completely after the CdSe dendron-nanocrystals reacted with
aminoethanol liquid for about 10 minutes at 100.degree. C., see
FIG. 8. The peaks appeared at about 1640 cm.sup.-1 and 1550
cm.sup.-1 in the spectrum of the resulting nanocrystals of the
coupling reaction are due to the secondary amide vibration modes,
which indicates the formation of the new amide bonds. The IR
spectra of the CdSe dendron-nanocrystals, either before or after
the ester coupling reactions, are nearly identical to those of
their corresponding free ligands, see FIG. 9. If
dendron-nanocrystals were terminated with --COOH groups, amide
coupling was accomplished through the traditional EDC coupling, and
similar IR results were observed.
[0057] The other requirement for biomedical applications is that
the DP-nanocrytal conjugates with biological functional groups in a
manner stable enough to withstand separation processes. The
separation and purification of dendron-nanocrystals can be carried
out by conventional techniques. Both CdSe and Au DP-nanocrystals
can pass through an adequate chromatography column readily. The
CdSe dendron-nanocrystals without any excess ligands were able to
stay in a Sephadex G-25 (or NAP.TM.-10) column with room light for
hours without leaving any residues after the nanocrystals run
through in a tight band. In contrast, the CdSe nanocrystals coated
by MPA were completely smeared and could not be washed out under
the same conditions.
[0058] The CdSe DP-nanocrystals can be purified and separated by
Gel-Electrophoresis without any excess ligands. The negatively
charged dendron-nanocrystals run toward the positive electrode. The
original ester terminated DP-nanocrystals did not move on the gel
because they were insoluble in water. In contrast, the two reaction
products were moved in two tight bands on the gel with
distinguishable mobilities. After gel-electrophoresis, the
DP-nanocrystals can be completely recovered back into pure water.
UV-Vis study revealed that the nanocrystals recovered from the gel
was unchanged. However, it is helpful to cover the gel
electrophoresis chamber during the electrophoresis to avoid the
room light radiation because of the strong oxidation environment in
the chamber. Coated with conventional single-chain thiol ligands,
both CdSe and Au nanocrystals cannot survive through the
separation/recovering process without a large excess of free thiol
ligands.
[0059] The coupling reactions presented here are common ones for
coupling functional organic/biological species onto solid
substrates although they have been unachievable for the CdSe and
other semiconductor nanocrystals coated by single-chain thiol
ligands without excess free ligands in the solution. The success of
these reactions show that these stabilized nanocrystals are
suitable labeling agents for various biomedical assays, such as
labels on antibodies for immunoassays and labels on polynucleotide
probes for polynucleotide hybridization assays. Similar to the
coupling reactions, gel electrophoresis has also been very
difficult to perform for semiconductor nanocrystals. Excess free
ligands were found necessary for the gel electrophoresis of
semiconductor and large-sized gold nanocrystals, and the
nanocrystals were often not recoverable.
[0060] The dendron ligands reported here have dramatically improved
the photochemical stability of nanocrystals.
[0061] If the resulting ligands generated by the photo-catalytic
oxidation occur on the surface of nanocrystals designed to be
insoluble in the solvent, the oxidized ligands will still surround
the inorganic core to form a micelle structure although there were
no chemical bonds between the ligands and the inorganic cores. If
the inorganic core is stable against photo-oxidation, the resulting
nanocrystal/ligand complex remains soluble and processable.
Insoluble ligand shells may be achievable for the dendron ligands
by inter-molecular cross-linking between the chains by multiple
hydrogen bonds, covalent bonds, or other relatively strong
interactions as described above. For the inorganic core, active
semiconductor and metal nanocrystals can be coated by another
inorganic component prior to the surface modification by dendron
ligands to make them photo-oxidation inactive.
[0062] Certain types of dendron ligands can presumably be used for
the synthesis of high quality semiconductor nanocrystals, provided
the recent discovery of many alternative routes towards high
quality semiconductor nanocrystals. With rationally designed
ligands, stable nanocrystals may be prepared with desired
functionality. The thiol based ligands described in this paper
cannot be used for the synthesis of high quality semiconductor
nanocrystals because thiols were found to be incompatible with the
existing synthetic schemes. Dendron ligands using carboxylic acid,
amine, phosphine oxide, or phosphonic acid groups as the
nanocrystal binding sites may be used for the direct synthesis of
high quality semiconductor nanocrystals and magnetic nanocrystals.
The thiol based dendrons presented in this invention may be applied
for the synthesis of stable noble metal nanocrystals using the
existing methods.
[0063] The inter- and intra-molecular chain tangling between the
branches of dendrons have played an important role for stabilizing
the semiconductor nanocrystals, in addition to the steric crowding
feature of the dendrons. Dendron ligands have may also be for the
synthesis of gold nanocrystals using different generations of
quinone-based (--C.dbd.O) hydrophobic dendrons with rigid branches
in hope to control the size of gold nanocrystals by the different
generation dendrons. The results indicated that the gold
nanocrystals synthesized with high generation dendrons have a
strong tendency to aggregate, which is different from the results
of this work. Their results may be caused by the rigid branches of
their dendrons, which cannot provide sufficient steric crowding on
the surface of nanocrystals and do not possess inter- and
intra-molecular chain tangling.
[0064] The cone-shaped structural feature and the single binding
site of a dendron ligand provides a better packing in the ligand
shell and an unambiguous orientation of the ligands on the surface
of nanocrystals.
[0065] The experimental results confirmed that the photochemical
stability of semiconductor and noble metal nanocrystal/ligand
complexes is the key for the development of reliable processing
chemistry for these nanocrystals. The surface-modification
chemistry of the nanocrystals with dendron ligands is simple and
straightforward. The thickness of the ligand layer of the
dendron-nanocrystals can be as thin as about 1 nm to achieve
substantial stability for those dendron-nanocrystals to be
manipulated as standard chemical reagents. The chemistry related to
CdSe dendron-nanocrystals can be applied for developing
photoluminescence-based labeling reagents using semiconductor
nanocrystals for biomedical applications. The chemistry presented
also provides an alternative path to apply noble metal nanocrystals
for chemical and biomedical applications. The invention also
creates many new opportunities in the field of colloidal
nanocrystals and related materials since it allows simple and
affordable processing chemistry. For example, stable magnetic
dendron-nanocrystals represent a new avenue for using magnetic
nanocrystals for drug delivery and enhanced magnetic resonance
imaging.
[0066] Those skilled in the art will appreciate that there are a
variety of dendron ligands not disclosed herein but would be
suitable for stabilizing many different types of colloidal
nanocrystals. It is preferable that the dendrons are not overly
bulky. It is desirable to have a relatively thin organic dendron
coating about the nanocrystal. An excessively thick dendron coating
will have deleterious effects on the electronic and structural
properties of the nanocrystals. Otherwise, any number of dendrons
may be used in the present invention. An important aspect of the
dendrons is that they are sufficiently bulky to sterically hinder
deleterious molecules.
[0067] Whereas, the present invention has been described in
relation to the drawings attached hereto, it should be understood
that other and further modifications, apart from those shown or
suggested herein, may be made within the spirit and scope of this
invention.
* * * * *